FDAJuly 1, 2019device

Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Calibration; it has been determined that the capnographs may have been calibrated during manufacturing using a lower than specified concentration of CO2

What to do

FDA enforcement status: Terminated

Brands named

carefusion 303carefusion

UPCs

10885403830013

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933 — Recall Details · AllClear